Sex differences in the Toll-like receptor-mediated response of plasmacytoid dendritic cells to HIV-1

被引:443
作者
Meier, Angela [1 ]
Chang, J. Judy [1 ]
Chan, Ellen S. [2 ]
Pollard, Richard B. [3 ]
Sidhu, Harlyn K. [1 ]
Kulkarni, Smita [4 ]
Wen, Tom Fang [1 ]
Lindsay, Robert J. [1 ]
Orellana, Liliana [2 ]
Mildvan, Donna [6 ]
Bazner, Suzane [1 ,7 ]
Streeck, Hendrik [1 ]
Alter, Galit [1 ]
Lifson, Jeffrey D. [5 ]
Carrington, Mary [4 ]
Bosch, Ronald J. [2 ]
Robbins, Gregory K. [7 ]
Altfeld, Marcus [1 ,7 ]
机构
[1] MIT, Massachusetts Gen Hosp, Ragon Inst, Boston, MA USA
[2] Harvard Univ, Sch Publ Hlth, Boston, MA 02115 USA
[3] Univ Calif Davis, Med Ctr, Sacramento, CA 95817 USA
[4] NCI, Canc & Inflammat Program, Expt Immunol Lab, Frederick, MD 21701 USA
[5] NCI, Sci Applicat Int Corp Frederick, AIDS & Canc Virus Program, Frederick, MD 21701 USA
[6] Beth Israel Deaconess Med Ctr, New York, NY 10003 USA
[7] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Div Infect Dis, Boston, MA USA
基金
美国国家卫生研究院; 英国医学研究理事会; 比尔及梅琳达.盖茨基金会;
关键词
IMMUNODEFICIENCY-VIRUS TYPE-1; IFN-ALPHA PRODUCTION; IMMUNE ACTIVATION; VIRAL LOAD; PROGNOSTIC VALUE; SIV INFECTION; RNA LEVELS; T-CELLS; I INTERFERON; SERUM-LEVELS;
D O I
10.1038/nm.2004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Manifestations of viral infections can differ between women and men(1), and marked sex differences have been described in the course of HIV-1 disease. HIV-1-infected women tend to have lower viral loads early in HIV-1 infection but progress faster to AIDS for a given viral load than men(2-7). Here we show substantial sex differences in the response of plasmacytoid dendritic cells (pDCs) to HIV-1. pDCs derived from women produce markedly more interferon-alpha (IFN-alpha) in response to HIV-1-encoded Toll-like receptor 7 (TLR7) ligands than pDCs derived from men, resulting in stronger secondary activation of CD8(+) T cells. In line with these in vitro studies, treatment-naive women chronically infected with HIV-1 had considerably higher levels of CD8(+) T cell activation than men after adjusting for viral load. These data show that sex differences in TLR-mediated activation of pDCs may account for higher immune activation in women compared to men at a given HIV-1 viral load and provide a mechanism by which the same level of viral replication might result in faster HIV-1 disease progression in women compared to men. Modulation of the TLR7 pathway in pDCs may therefore represent a new approach to reduce HIV-1-associated pathology.
引用
收藏
页码:955 / U161
页数:6
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